The Hb E (HBB: c.79G&gt;A), Mean Corpuscular Volume, Mean Corpuscular Hemoglobin Cutoff Points in Double Heterozygous Hb E/– –<sup>SEA</sup>α-Thalassemia-1 Carriers are Dependent on Hemoglobin Levels

© 2017 Informa UK Limited, trading as Taylor & Francis Group. Identifying double heterozygosities in Hb E (HBB: c.79 G > A)/– – SEA (Southeast Asian) (α-thalassemia-1) (α-thal-1) in patients first diagnosed as carrying Hb E is important in thalassemia control. Low Hb E, mean corpuscular vol...

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Main Authors: Prapapun Leckngam, Ektong Limweeraprajak, Tiemjan Kiewkarnkha, Thanusak Tatu
Format: Journal
Published: 2018
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/46446
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spelling th-cmuir.6653943832-464462018-04-25T07:28:48Z The Hb E (HBB: c.79G&gt;A), Mean Corpuscular Volume, Mean Corpuscular Hemoglobin Cutoff Points in Double Heterozygous Hb E/– –<sup>SEA</sup>α-Thalassemia-1 Carriers are Dependent on Hemoglobin Levels Prapapun Leckngam Ektong Limweeraprajak Tiemjan Kiewkarnkha Thanusak Tatu Agricultural and Biological Sciences © 2017 Informa UK Limited, trading as Taylor & Francis Group. Identifying double heterozygosities in Hb E (HBB: c.79 G > A)/– – SEA (Southeast Asian) (α-thalassemia-1) (α-thal-1) in patients first diagnosed as carrying Hb E is important in thalassemia control. Low Hb E, mean corpuscular volume (MCV) and mean corpuscular hemoglobin (Hb) (MCH) levels have been observed in this double heterozygosity. However, the cutoff points of these parameters have never been systematically established. Here, we analyzed Hb E and red blood cell (RBC) parameters in 372 Hb E patients grouped by Hb levels, by the status of–– SEA and –α 3.7 (α-thal-2; rightward) deletions, to establish the cutoff points. Then, the established cutoff points were evaluated in 184 Hb E patients. It was found that the cutoff points of Hb E, MCV, MCH were significantly dependent on the Hb levels. In the group having Hb levels < 10.0 g/dL, the cutoff points of Hb E, MCV and MCH were 21.2%, 64.9 fL and 21.0 pg, respectively, and were 25.6%, 72.8 fL and 23.9 pg, respectively, in the group having Hb levels 10.0–11.9 g/dL. Finally, in the group having Hb levels ≥12.0 g/dL, the cutoff points of Hb E, MCV and MCH were 27.1%, 76.7 fL and 25.3 pg, respectively. Thus, to screen for the double heterozygous Hb E/– – SEA anomaly in patients initially diagnosed as carrying Hb E, the Hb levels must be taken into account in choosing the suitable cutoff points of these three parameters. 2018-04-25T06:55:00Z 2018-04-25T06:55:00Z 2017-01-02 Journal 1532432X 03630269 2-s2.0-85017521053 10.1080/03630269.2017.1295984 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85017521053&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/46446
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Agricultural and Biological Sciences
spellingShingle Agricultural and Biological Sciences
Prapapun Leckngam
Ektong Limweeraprajak
Tiemjan Kiewkarnkha
Thanusak Tatu
The Hb E (HBB: c.79G&gt;A), Mean Corpuscular Volume, Mean Corpuscular Hemoglobin Cutoff Points in Double Heterozygous Hb E/– –<sup>SEA</sup>α-Thalassemia-1 Carriers are Dependent on Hemoglobin Levels
description © 2017 Informa UK Limited, trading as Taylor & Francis Group. Identifying double heterozygosities in Hb E (HBB: c.79 G > A)/– – SEA (Southeast Asian) (α-thalassemia-1) (α-thal-1) in patients first diagnosed as carrying Hb E is important in thalassemia control. Low Hb E, mean corpuscular volume (MCV) and mean corpuscular hemoglobin (Hb) (MCH) levels have been observed in this double heterozygosity. However, the cutoff points of these parameters have never been systematically established. Here, we analyzed Hb E and red blood cell (RBC) parameters in 372 Hb E patients grouped by Hb levels, by the status of–– SEA and –α 3.7 (α-thal-2; rightward) deletions, to establish the cutoff points. Then, the established cutoff points were evaluated in 184 Hb E patients. It was found that the cutoff points of Hb E, MCV, MCH were significantly dependent on the Hb levels. In the group having Hb levels < 10.0 g/dL, the cutoff points of Hb E, MCV and MCH were 21.2%, 64.9 fL and 21.0 pg, respectively, and were 25.6%, 72.8 fL and 23.9 pg, respectively, in the group having Hb levels 10.0–11.9 g/dL. Finally, in the group having Hb levels ≥12.0 g/dL, the cutoff points of Hb E, MCV and MCH were 27.1%, 76.7 fL and 25.3 pg, respectively. Thus, to screen for the double heterozygous Hb E/– – SEA anomaly in patients initially diagnosed as carrying Hb E, the Hb levels must be taken into account in choosing the suitable cutoff points of these three parameters.
format Journal
author Prapapun Leckngam
Ektong Limweeraprajak
Tiemjan Kiewkarnkha
Thanusak Tatu
author_facet Prapapun Leckngam
Ektong Limweeraprajak
Tiemjan Kiewkarnkha
Thanusak Tatu
author_sort Prapapun Leckngam
title The Hb E (HBB: c.79G&gt;A), Mean Corpuscular Volume, Mean Corpuscular Hemoglobin Cutoff Points in Double Heterozygous Hb E/– –<sup>SEA</sup>α-Thalassemia-1 Carriers are Dependent on Hemoglobin Levels
title_short The Hb E (HBB: c.79G&gt;A), Mean Corpuscular Volume, Mean Corpuscular Hemoglobin Cutoff Points in Double Heterozygous Hb E/– –<sup>SEA</sup>α-Thalassemia-1 Carriers are Dependent on Hemoglobin Levels
title_full The Hb E (HBB: c.79G&gt;A), Mean Corpuscular Volume, Mean Corpuscular Hemoglobin Cutoff Points in Double Heterozygous Hb E/– –<sup>SEA</sup>α-Thalassemia-1 Carriers are Dependent on Hemoglobin Levels
title_fullStr The Hb E (HBB: c.79G&gt;A), Mean Corpuscular Volume, Mean Corpuscular Hemoglobin Cutoff Points in Double Heterozygous Hb E/– –<sup>SEA</sup>α-Thalassemia-1 Carriers are Dependent on Hemoglobin Levels
title_full_unstemmed The Hb E (HBB: c.79G&gt;A), Mean Corpuscular Volume, Mean Corpuscular Hemoglobin Cutoff Points in Double Heterozygous Hb E/– –<sup>SEA</sup>α-Thalassemia-1 Carriers are Dependent on Hemoglobin Levels
title_sort hb e (hbb: c.79g&gt;a), mean corpuscular volume, mean corpuscular hemoglobin cutoff points in double heterozygous hb e/– –<sup>sea</sup>α-thalassemia-1 carriers are dependent on hemoglobin levels
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85017521053&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/46446
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